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血清肌酸激酶同工酶MB活性:采用琼脂糖凝胶电泳加滤纸荧光扫描试剂盒的评估

Serum creatine kinase isoenzyme MB activity: evaluation of a kit employing agarose-gel electrophoresis with overlay paper fluorescence scanning.

作者信息

Hamilton S R, Wimsatt T, Torrieri R, Rock R C

出版信息

Clin Chim Acta. 1979 Feb 1;91(3):285-94. doi: 10.1016/0009-8981(79)90485-6.

Abstract

A commercial kit for determining serum creatine kinase isoenzyme MB activity was evaluated. The kit employed agarose-gel electrophoresis followed by incubation of overlay paper on the agarose and then fluorescnece scanning of the paper. Within-day coefficients of variation ranged from 24.9% for a specimen with no elevation of MB activity of 6.6% for a specimen with moderately elevated MB activity. The kit appeared to demonstrate MB in all sera and showed higher than expected values in recovery studies. The kit performed in a relatively linear fashion from 50 to 500 I.U./l total creatine kinase activity. Hemolysis appeared to lower measured MB. For comparison with another method, specimens were also analyzed by microcolumn chromatography, which was found to incompletely separate isoenzymes. The kit produced lower values than microchromatography for specimens with low MB activities and higher values for specimens with elevated MB activities. Patients without corroborative evidence of myocardial injury showed a somewhat hyperbolic relationship between per cent MB and total creatine kinase activity, but MB activity was generally 4 I.U./l or less. Although the kit had serious laboratory shortcomings, it may be as clinically useful as other methodologies.

摘要

对一种用于测定血清肌酸激酶同工酶MB活性的商用试剂盒进行了评估。该试剂盒采用琼脂糖凝胶电泳,随后将覆盖纸在琼脂糖上孵育,然后对纸张进行荧光扫描。日内变异系数范围为:MB活性无升高的标本为24.9%,MB活性中度升高的标本为6.6%。该试剂盒似乎能在所有血清中检测到MB,并且在回收率研究中显示出高于预期的值。该试剂盒在总肌酸激酶活性为50至500 I.U./l时以相对线性的方式运行。溶血似乎会降低测得的MB。为了与另一种方法进行比较,还通过微柱色谱法对标本进行了分析,发现该方法不能完全分离同工酶。对于MB活性低的标本,该试剂盒产生的值低于微柱色谱法;对于MB活性升高的标本,该试剂盒产生的值高于微柱色谱法。没有心肌损伤的确证证据的患者,MB百分比与总肌酸激酶活性之间呈现出某种双曲线关系,但MB活性通常为4 I.U./l或更低。尽管该试剂盒存在严重的实验室缺陷,但它在临床上可能与其他方法一样有用。

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